when carbon dioxide gas is collected down ward of water wet gas is collected by the downward displacement of water . This is used for gases that are not very soluble in water . ... In water , carbon dioxide produces a weakly acidic solution , carbonic acid .
Answer:
∴ Fractional distillation is the technique used to separate the fraction
Explanation:
A: Refinery gas
B: Gasoline fraction
C: Naphtha
D: Kerosene
E: Diesel Oil
F: Fuel oil fraction
G: Lubricating fraction
H: Bitumen
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
The chemical formula does not show how the atoms are connected to one another.
When we write the chemical formula of any substance, we are not able to understand the spatial arrangement of that substance's atoms. This is extremely important in organic compounds, which exhibit different physical characteristics as well as different chemical characteristics due to the way their atoms are arranged in space. These isomers are known as enantiomers.